Monica Poscente

1.8k total citations
10 papers, 106 citations indexed

About

Monica Poscente is a scholar working on Molecular Biology, Genetics and Genetics. According to data from OpenAlex, Monica Poscente has authored 10 papers receiving a total of 106 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Molecular Biology, 5 papers in Genetics and 2 papers in Genetics. Recurrent topics in Monica Poscente's work include Genomic variations and chromosomal abnormalities (3 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (2 papers) and Urological Disorders and Treatments (2 papers). Monica Poscente is often cited by papers focused on Genomic variations and chromosomal abnormalities (3 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (2 papers) and Urological Disorders and Treatments (2 papers). Monica Poscente collaborates with scholars based in Italy, Lebanon and Spain. Monica Poscente's co-authors include Paola Grammatico, Carmelilia De Bernardo, Rita Rinaldi, Barbara Grammatico, Maria G. Matera, Vito Michele Fazio, Emanuela Massi, Monica Rinaldi, Wim Wuyts and M Assumma and has published in prestigious journals such as European Journal of Nuclear Medicine and Molecular Imaging, Journal of Pediatric Surgery and Genes Chromosomes and Cancer.

In The Last Decade

Monica Poscente

9 papers receiving 94 citations

Peers

Monica Poscente

GENET

RHEUM

PRM

Sonia Canún Mexico

Pauline Marzin France

Chuanhua Fu United States

Yonit A. Addissie United States

Flore Zufferey Switzerland

Nadja Kokalj Vokač Slovenia

Katherine A. Bosanko United States

Virginie Laugel-Haushalter France

Sandhya Parkash Canada

Regan Klatt Canada

Sonia Canún Mexico

Monica Poscente

97 ×2.2

GENET

7 ×0.2

RHEUM

86 ×2.7

15 ×0.7

PRM

13 ×0.6

Citations per year, relative to Monica Poscente Monica Poscente (= 1×) peers Sonia Canún

Countries citing papers authored by Monica Poscente

Since Specialization

Citations

This map shows the geographic impact of Monica Poscente's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Monica Poscente with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Monica Poscente more than expected).

Fields of papers citing papers by Monica Poscente

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Monica Poscente. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Monica Poscente. The network helps show where Monica Poscente may publish in the future.

Co-authorship network of co-authors of Monica Poscente

This figure shows the co-authorship network connecting the top 25 collaborators of Monica Poscente. A scholar is included among the top collaborators of Monica Poscente based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Monica Poscente. Monica Poscente is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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10 of 10 papers shown

Poscente, Monica, Doron Tolomeo, A. L’Abbate, et al.. (2024). Aggressive systemic mastocytosis with the co-occurrence of PRKG2::PDGFRB, KAT6A::NCOA2, and RXRA::NOTCH1 fusion transcripts and a heterozygous RUNX1 frameshift mutation. Cancer Genetics. 284-285. 5–11. 1 indexed citations

Magini, Pamela, Monica Poscente, Simona Ferrari, et al.. (2015). Cytogenetic and molecular characterization of a recombinant X chromosome in a family with a severe neurologic phenotype and macular degeneration. Molecular Cytogenetics. 8(1). 58–58. 15 indexed citations

Signori, Emanuela, Emanuela Massi, Maria G. Matera, et al.. (2007). A combined analytical approach reveals novel EXT1/2 gene mutations in a large cohort of Italian multiple osteochondromas patients. Genes Chromosomes and Cancer. 46(5). 470–477. 39 indexed citations

Rinaldi, Rita, P. Parisi, Monica Poscente, Menotti Calvani, & Paola Grammatico. (2004). Attention-deficit/hyperactivity disorder, speech delay and polymicrogyria associated with trisomy 18 mosaicism.. PubMed. 15(3). 379–82.

Marrocco, Giacinto, Monica Poscente, Silvia Majore, et al.. (2003). Clinical management and molecular cytogenetic characterization in a 45,X/46,X,idic(Yp) patient with severe hypospadia. Journal of Pediatric Surgery. 38(8). 1258–1262. 9 indexed citations

Rinaldi, Rita, Carmelilia De Bernardo, M Assumma, et al.. (2003). Cytogenetic and molecular characterization of a de novo 4q24qter duplication and correlation to the associated phenotype. American Journal of Medical Genetics Part A. 118A(2). 122–126. 24 indexed citations

Liberatore, Mauro, et al.. (2003). The effects of 99m Tc-HMPAO-labelled leucocyte scan on human karyotype. European Journal of Nuclear Medicine and Molecular Imaging. 30(10). 1365–1370. 6 indexed citations

Poscente, Monica, Patrizia Lulli, M Morellini, et al.. (2000). TNFA gene: the -308 promoter polymorphism in migraine. The Journal of Headache and Pain. 1(S2). S169–S171. 6 indexed citations

Grammatico, Paola, Silvia Majore, Giacinto Marrocco, et al.. (1999). 46,XX,der(2)t(2;10)(2pter-->2q37::10p13-->10pter)[127]/45,X,der(2)t(2;10) (2pter-->2q37::10p13-->10pter)[23]. Karyotype-phenotype correlation and genetic counselling in complex karyotypes.. PubMed. 10(4). 351–8. 3 indexed citations

10.

Grammatico, Paola, et al.. (1996). Trisomy 20 in a papillary urothelial carcinoma of the ureter. Cancer Genetics and Cytogenetics. 90(2). 132–134. 3 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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